EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS134-12045 
Organism
Homo sapiens 
Tissue/cell
Mesendoderm 
Coordinate
chr11:126016000-126018170 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs111977000chr11126017059hg19
TF binding sites/motifs
Number: 30             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr11:126017058-126017076CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:126017062-126017080CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:126017099-126017117CCCTCCCTCCCTCCCTCC-6.03
EWSR1-FLI1MA0149.1chr11:126017088-126017106CCTGTCTTCCTCCCTCCC-6.04
EWSR1-FLI1MA0149.1chr11:126017092-126017110TCTTCCTCCCTCCCTCCC-6.36
EWSR1-FLI1MA0149.1chr11:126017084-126017102CTTTCCTGTCTTCCTCCC-6.38
EWSR1-FLI1MA0149.1chr11:126017122-126017140CTTTCCTCCCTCCCTCCC-6.42
EWSR1-FLI1MA0149.1chr11:126017117-126017135CCTTCCTTTCCTCCCTCC-6.94
EWSR1-FLI1MA0149.1chr11:126017067-126017085CCTCCCTCCCTCCCTTCC-7.08
EWSR1-FLI1MA0149.1chr11:126017071-126017089CCTCCCTCCCTTCCTTTC-7.08
EWSR1-FLI1MA0149.1chr11:126017051-126017069CCTTCCTCCCTCCCTCCC-7.28
Foxd3MA0041.1chr11:126017775-126017787AAACAAACAAAC-6.32
NR2C2MA0504.1chr11:126017856-126017871TGACCTTTGACCTGG-7.36
Nr2f6MA0677.1chr11:126017856-126017870TGACCTTTGACCTG-7.73
RxraMA0512.2chr11:126017856-126017870TGACCTTTGACCTG-7.58
ZNF263MA0528.1chr11:126017110-126017131TCCCTCCCCTTCCTTTCCTCC-6.18
ZNF263MA0528.1chr11:126017105-126017126CTCCCTCCCTCCCCTTCCTTT-6.2
ZNF263MA0528.1chr11:126016404-126016425GCCCCTTCCCTCACCTCCTCC-6.51
ZNF263MA0528.1chr11:126017067-126017088CCTCCCTCCCTCCCTTCCTTT-6.54
ZNF263MA0528.1chr11:126017121-126017142CCTTTCCTCCCTCCCTCCCTC-6.89
ZNF263MA0528.1chr11:126017125-126017146TCCTCCCTCCCTCCCTCCCTA-6.89
ZNF263MA0528.1chr11:126016445-126016466TCCCCCACCCCCTCATCCCTC-6.94
ZNF263MA0528.1chr11:126017062-126017083CCCTCCCTCCCTCCCTCCCTT-7.05
ZNF263MA0528.1chr11:126017113-126017134CTCCCCTTCCTTTCCTCCCTC-7.11
ZNF263MA0528.1chr11:126017050-126017071CCCTTCCTCCCTCCCTCCCTC-7.19
ZNF263MA0528.1chr11:126017117-126017138CCTTCCTTTCCTCCCTCCCTC-7.48
ZNF263MA0528.1chr11:126017099-126017120CCCTCCCTCCCTCCCTCCCCT-7.54
ZNF263MA0528.1chr11:126017058-126017079CCCTCCCTCCCTCCCTCCCTC-7.97
ZNF263MA0528.1chr11:126017054-126017075TCCTCCCTCCCTCCCTCCCTC-8.08
ZNF263MA0528.1chr11:126017095-126017116TCCTCCCTCCCTCCCTCCCTC-8.08
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr11126016000126016400
chr11126016400126017400
chr11126017631126017949
Number: 1             
IDChromosomeStartEnd
GH11I126145chr11126015848126018967
Enhancer Sequence
TCTCGGGGAA GTGTTCTGTG CCAGGGGTCT ACTTCAGCCC CCTGTTCTGG GTGCTGCCTC 60
GAAGGCCAGT CCCTCTGGGA TGTGTGTTGG GACGGGGATT GGGTGAGCAC CCTGGGCCTT 120
GGCAGGTGAG GTCATTCACC TCTCCTTCTC TGAGGGACTT CTGGAAACTT GAGGCATCCT 180
CTGAGCAGCG TCGTTCCTGC CCTTACTTGG TCAGGAAGCT GTGATGCAGC CCAGAGACCC 240
CCTAGTCCTT TCCTCCCCCC ACTCTCCTCT CTGTGTACCT TGAGCACAAA CACTCGGAGA 300
GCTCCTGGAG AGACGAGTTC CAGCAGGAAG CAGGGGGTGT CCTGGGGGCC CAGAGAGAGA 360
AGGCCCTGTC GTCTGTGGGG GCCACAGGTC TCCACCCGTG CTCAGCCCCT TCCCTCACCT 420
CCTCCCATCT TCCTCAGGAT CCCGCTCCCC CACCCCCTCA TCCCTCTGCA CAGACCTGCC 480
AAGTTTGGGA CATGAGAACA GGCCAGGTCC CCTCTGGGGA GCCCGGGGTG GGCGGAGCCA 540
GGCCTGGCTG GGCCTCCAGG TTGGCCTGCC CTGGCCCCTG GGTTTAATAA ACTCCGAGAG 600
AGGTTTTCAA AGGCCACTTG ATCTTCCCCA TCAGGCAGCC CCTGTCTCCC TTTCAGAGCC 660
GCGGGACTGG AAAGAAAAAA CCGCTCAATG AACAAGGCGG CCAGAGAAAG CTGAGCTGCG 720
GGGCACCTTC TATGAATTTC TGATGAGCCC ACGGCCCTGA CTCCTGGGTC CCGGCCCGGT 780
GCAGTCAGGG ATGTTAGTTT AAGTCATTTC GCACGGTTCA CTGGCTCTCT GAGAGCAGCT 840
TGTCTCCAGC CTGGGCCTCT CTAACAAGCT CTTTTTACTC AGGGCTTCTC TGAGCATAGA 900
CCTCAAACAA TAGCAGCTTT CAAGGGGCTC GGCCCTCCTC TGGCGGCCTC CCTCTCCCAA 960
CCCCAGCCAA GCCCAGCCTC TATCGCTCAC TGCCCACCTG AGCGCCCCCA CCCACAGCCT 1020
GACCCGCAGC GGCATTCAGG GAAGACTCGC CCCTTCCTCC CTCCCTCCCT CCCTCCCTCC 1080
CTTCCTTTCC TGTCTTCCTC CCTCCCTCCC TCCCTCCCCT TCCTTTCCTC CCTCCCTCCC 1140
TCCCTACTGC CCCTGCCCTT TCTTGCTGTA AACAGGGCAG GAGTGCGCAG TGGGGCTCTC 1200
AGGAGCAGGC CACACTGCCA CGCAACTCTA GAACACTGTG TGGATGGCAC CCCCTGGGGT 1260
TGTGCAATGA AGAGCCCCCA GTAGAACGCA GCTCATTCCA ACACTCTAAG CCTATTGGGC 1320
TCCTCAGCCC TCTTGAAACT GAGCAGTTTC CTCCTCCCTT TAGTCCAAGG AGGGAGCTGG 1380
CTTCCTCCAC ACTGCAGGCT GTCACCTGCC CCGCAGGACC CAGACCTGGT GGGGTTGATG 1440
GAGTTGCCTC CAAGAAGCGT GAAGCCGGCT CGGAGCACCT CTAGTGCCCA AGCCTGAGAG 1500
CGGACATTGG CGGCAGCGTC CCCCTGCAGA GGGGCTCCCC AGACACCAGA GGGACCGTGG 1560
CTCTCATCAG TCCAGGCCTC TCTATCTTCC CCATTCCCAC TGTTCTCCAC TGTCCCCCCT 1620
GTTCCTCAGA GCAGTGATGA GACAACTTCC AGTCCTCCCT ACCTGCCTCT GGCCTTCTTG 1680
CTCGCTAAGG GGTCTTAGGA AGAGACTCCT GGGAAGAGGT TCATTAATCA GCAGATGAGT 1740
CATTTACATG TTTAGACTAG ACCTCTGGCC AAAGCAAACA AACAAACAAA GTTCATATTG 1800
AGACAAGTCA ATATTTGACT TAATGAGAGT GCCTTGCCAG TTGAATGCTT TGATGGTGAC 1860
CTTTGACCTG GGAGCTTTGG AAGGCATTTG AGCTGCAGTC CCATGGACAC TGCACTTTGG 1920
GAGGGGCTCC AGCCCCACTC CTACAGCACC TGCCAGCAAT TAAGTTTCCC TCCCCAGGGA 1980
TCTAGGCCCT GCCTCTGGGG CCATGGGGTC TCTCACCTTT CAGGAGTCCC AGGCAGCCCA 2040
GGACTTCTTT CTTTCTGGAA GCTGCTAGAG AAAGCCCAGT TTCATGTCCC CTTTGCAAAC 2100
CCCCCCACGC TAATAACTCA CCTTCTTCAG GAAGTGAAGT CTGATCAGAG ACAGCCTGGC 2160
AAGAGGAAAG 2170